Threatened abortion. Haemorrhage specified as due to threatened abortion
Conditions
Interventions
Intervention 1: Control group: They received 400 mg of progesterone suppository (Cyclogest®) with abstinence from sexual intercourse and physical exertion. Progesterone was used daily until two days o
Sponsors
Vice Chancellor for research, School of Traditional medicine, Tehran University of Medical Scienc
Eligibility
Sex/Gender
Female
Age
12 Years to 55 Years
Inclusion criteria
Inclusion criteria: Pregnant women presenting with mild to moderate vaginal bleeding (using 2 Pads or less per day) Up to 16 weeks of pregnancy Normal ultrasound (including a normal gestational sac at five wk of gestation, yolk sac at six wk, or fetal heart activity at seven wk of gestation or later) Closed cervix in vaginal examination Singleton pregnancy Having consent to participate in the study Tendency to consume this special food (in intervention group) No fried eggs with grape molasses in routine diet food
Exclusion criteria
Exclusion criteria: Mother systemic illness such as fever, diabetes, chronic hypertension History of recurrent miscarriage Heavy vaginal bleeding (>2 pads soaked) Loss of conception tissue Open cervix (>2 centimeters) in vaginal examination Cervical lesions such as polyps or cervicitis Abnormal findings on ultrasound (absence of a normal gestational sac at 5 weeks gestational age, a yolk sac or cardiac activity at 7 weeks gestational age, incomplete abortion, missed abortion) Multiple gestation sacs Molar pregnancy Fetal or uterine anomalies Allergy or intolerance to eggs, grape molasses or progesterone The patient withdrew from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine the miscarriage rate (loss of an intrauterine pregnancy at =20 week’s gestation) in patients with threatened abortion. Timepoint: Weekly follow-up until vaginal bleeding has been stopped And follow-up at 20 weeks of pregnancy. Method of measurement: Self-designed form. | — |
Secondary
| Measure | Time frame |
|---|---|
| The average duration of vaginal bleeding. Timepoint: Weekly follow-up until vaginal bleeding has been stopped And follow-up at 20 weeks of pregnancy. Method of measurement: Self-designed form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Fatemeh Moradi
Tehran University of Medical Sciences
Outcome results
None listed